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The Associate Specialist Technical Applications Group (TAG) supports the development, formulation, scale-up, and commercialization of nutritional and solid dose products, including capsules and tablets. This entry-level, hands-on role works across laboratory and manufacturing environments to support industrial trials, troubleshooting, data analysis, and technology transfer, partnering with cross-functional teams to ensure successful product implementation and compliance with quality and regulatory standards.
Job Responsibility
Support formulation development, evaluation, and process improvement for nutritional and solid dose products
Execute laboratory studies, development trials, and assist with industrial trials and production support
Collect, analyze, and report data
prepare technical summaries and documentation
Support scale-up, validation, and technology/process transfer to internal and external manufacturing sites
Provide technical support for manufacturing, including troubleshooting, process improvements, and cost savings initiatives
Create and maintain technical documentation (raw material specifications, batch records, change controls, deviations, transfer documents)
Maintain laboratory records, equipment, and workspaces
Identify and support continuous improvement initiatives and elimination of non-value-added activities
Research and share scientific and technical information with the team
Perform documentation review and audits to ensure accuracy and compliance with SOPs, GLP, and cGMP standards
Support change control activities and track project approvals
Collaborate cross-functionally (Manufacturing, Quality Assurance, Quality Control, Regulatory, Procurement) to ensure compliance and resolve issues
Requirements
Bachelor's degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Food Science, or related scientific discipline
0–1 year of relevant experience (internships, co-ops, or entry-level experience considered)
Basic understanding of formulation development and manufacturing processes
Familiarity with laboratory or manufacturing environments and nutraceutical, pharmaceutical, or consumer health products
Working knowledge of GLP and cGMP practices
Proficiency with Microsoft Office (Word and Excel)
Strong technical writing and documentation skills
Knowledge of scientific principles related to formulation and manufacturing processes
Ability to work in environments with exposure to powders, chemicals, and allergens